Prematurity-Related Ventilatory Control: Role in Respiratory Outcomes (Pre-Vent) - Catalog

  • Name

    Prematurity-Related Ventilatory Control: Role in Respiratory Outcomes (Pre-Vent)

  • Accession Number

    HLB03082626a

  • Acronym

    Pre-Vent

  • Related studies
  • BSI Study IDs

    PRV

  • Is public use dataset

    False

  • Keywords

    Obstetric Labor, Premature

    Obstetric Labor Complications

    Pregnancy Complications

    Female Urogenital Diseases and Pregnancy Complications

    Urogenital Diseases

    Premature Birth

  • Ingestion Status
    Released
  • Has Study Datasets

    True

  • Has Specimens

    True

  • Specimen ID Type
    Coded
  • Study Website
  • The Framingham Heart Study Group requires that the requestor must obtain full or expedited IRB/Ethics Committee review and approval to obtain these data. Waivers or a determination that the research is exempt from ethical regulations do not suffice.

    False

  • Clinical Trial URLs
  • Study type
    Epidemiology Study
  • Collection Type
    Open BioLINCC Study
  • Cohort type
    Pediatric
  • Interventions
  • Study Open Date (Data)

    2026-05-07

  • Study Open Date (Specimens)

    2026-05-07

  • Date materials available

    2025-04-03

  • Last updated

    None

  • Study period

    March 2018 – June 2021

  • Study Contacts
  • NHLBI Division

    DLD

  • Classification
    Lung
  • HIV study classification
    non-HIV
  • COVID study classification
    non-COVID
  • Pre-Website # of Specimens Shipped

    None

  • # of Returned Specimens

    None

  • Primary Publication URLs
  • Conditions
    Infant, Premature
    Prematurity
  • Objectives

    To develop a predictive model of short-term respiratory outcomes in extremely preterm infants, based on quantitative analysis of neonatal ICU cardiorespiratory monitoring data.

  • Background

    Preterm birth is a major cause of infant mortality and morbidity worldwide and a leading contributor to disability. Abnormal control of breathing is common in preterm infants and usually manifests as apnea, intermittent hypoxemia, bradycardia, and periodic breathing. Extremely preterm infants may also have impaired gas exchange caused by respiratory distress syndrome and subsequent bronchopulmonary dysplasia. The combination of apnea and lung disease often leads to more prolonged episodes of intermittent hypoxia. Such chronic intermittent hypoxia is associated with worse short-term outcomes (e.g., increased respiratory support, retinopathy of prematurity) and neurodevelopmental impairment that are difficult to predict in the neonatal ICU (NICU). The contribution of abnormal control of breathing to respiratory outcomes has not been determined. The Pre-Vent study was initiated to analyze cardiorespiratory continuous waveform monitoring data to delineate mechanisms of immature ventilatory control in preterm infants and identify predictive markers.

  • Participants

    Infants less than 29 weeks gestational age with continuously archived cardiorespiratory monitoring data were included. 717 total infants were evaluated.

  • Design

    Pre-Vent was an observational multicenter prospective cohort study. Clinical data collected included respiratory support, medications, and co-morbidity data. Physiologic data consisted of variables extracted from cardiorespiratory monitoring data and quantified by count of events per day and duration per event. The extracted variables were apnea (≥20 seconds), periodic breathing (wavelet transform using a five-breath template), intermittent hypoxia events with oxygen saturation <80% as measured by pulse oximetry, intermittent hypoxia events with oxygen saturation <90% as measured by pulse oximetry, and bradycardia (<80bpm for 5 seconds or longer).


    Infants discharged prior to 40 weeks post-menstrual age or inpatient infants at 40 weeks post-menstrual age had a favorable outcome if they were not on respiratory support or respiratory medications. Infants discharged prior to 40 weeks post-menstrual age or inpatient infants at 40 weeks post-menstrual age had an unfavorable outcome if they were on respiratory medications and/or respiratory support, or deceased.

  • Conclusions

    The major findings of this study were that mathematical models based on cardiorespiratory bedside monitoring can identify alterations in physiologic measures that are independently associated with unfavorable respiratory outcomes in extremely preterm infants. Both physiologic and clinical variables contributed to good prediction models, with the contribution by physiologic variables increasing with postnatal age.


    Weese-Mayer DE, Di Fiore JM, Lake DE, et al. Maturation of cardioventilatory physiological trajectories in extremely preterm infants. Pediatr Res. 2024;95(4):1060-1069. doi:10.1038/s41390-023-02839-0


    Ambalavanan N, Weese-Mayer DE, Hibbs AM, et al. Cardiorespiratory Monitoring Data to Predict Respiratory Outcomes in Extremely Preterm Infants. Am J Respir Crit Care Med. 2023;208(1):79-97. doi:10.1164/rccm.202210-1971OC

  • Disease classification
  • Publications
  • Mat types
    DNA
  • Network

The study population available in BioLINCC study data may be lower than total study enrollment due to Informed Consent restrictions and other factors.

  • Subjects

    There are 730 participants.


    Last Modified: May 29, 2026, 11:42 a.m.
  • Age

    Preterm infants.


    Last Modified: May 29, 2026, 11:42 a.m.
  • Sex

     

    Total Subjects

    Female

    357

    Male

    373


    Last Modified: May 29, 2026, 11:42 a.m.
  • Race

     

    Total Subjects

    <missing>

    691

    Unknown/Declined to self-identify

    19

    Black

    8

    White

    11

    American Indian/Native Alaskan/Asian/Other

    *S

    *Values has been suppressed due to low counts.


    Last Modified: May 29, 2026, 11:42 a.m.

Please note that biospecimen availability is subject to review by the NHLBI, BioLINCC, and the NHLBI Biorepository. Certain biospecimens may not be made available for your request. The BioLINCC Users Guide describes the components of the review process.

  • Material Types

    DNA


    Last Modified: May 29, 2026, 11:42 a.m.
  • General Freeze/Thaw Status

    The vast majority of samples are unthawed.


    Last Modified: May 29, 2026, 11:42 a.m.
  • Visits (Vials)

    Updated 29th May 2026.

    DNA

    Total

    252

    252


    Last Modified: May 29, 2026, 11:42 a.m.
  • Visits (Subjects)

    Updated 29th May 2026.

     

    DNA vials are unquantified.

    Material

    DNA

    Total number of subjects

    Average vials per subject

    136

    1.85


    Last Modified: May 29, 2026, 11:42 a.m.